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Chembiochem : a European Journal of Chemical Biology|August 23, 2022
Extending the Structure-Activity Relationship of Disorazole C1 : Exchanging the Oxazole Ring by Thiazole and Influence of Chiral Centers within the Disorazole Core on CytotoxicityLuca Lizzadro, Oliver Spieß, Wera Collisi, et al.
Molecules (Basel, Switzerland)|March 13, 2024
Synthesis of a Non-Symmetrical Disorazole C1-Analogue and Its Biological ActivityLuca Lizzadro, Oliver Spieß, Silke Reinecke, et al.
The Journal of Biological Chemistry|December 15, 2010
Cloning and characterization of an Armillaria gallica cDNA encoding protoilludene synthase, which catalyzes the first committed step in the synthesis of antimicrobial melleolidesBenedikt Engels, Uwe Heinig, Torsten Grothe, et al.
Fungal Biology|October 15, 2010
Lepraric acid derivatives as chemotaxonomic markers in Hypoxylon aeruginosum, Chlorostroma subcubisporum and C. cyaninum, sp. novThomas Laessøe, Prasert Srikitikulchai, Jacques Fournier, et al.
ACS Omega|April 29, 2024
Comparative Study of Toxic Terpenoidal Aldehydes and Lactone Derivatives from the European Polypore Bondarzewia mesentericaWinnie Chemutai Sum, Sherif S Ebada, Harald Kellner, et al.
Chemistry & Biodiversity|September 19, 2024
p-Terphenyl and Orsellinic Acid Derivatives from the European Polyporales Terana coerulea and Sparassis brevipesWinnie Chemutai Sum, Sherif S Ebada, Harald Kellner, et al.
Journal of Natural Products|February 17, 2022
Terpenoids and Meroterpenoids from Cultures of Two Grass-Associated Species of Amylosporus (Basidiomycota)Blondelle Matio Kemkuignou, Ashaimaa Y Moussa, Cony Decock, et al.
Fungal Biology|February 18, 2014
Hypoxyvermelhotins A-C, new pigments from Hypoxylon lechatii sp. novEric Kuhnert, Simone Heitkämper, Jacques Fournier, et al.
Natural Product Reports|August 8, 2025
Coprophilous fungi in the search for new antimicrobials and other beneficial natural productsEsteban Charria-Girón, Joseph Tchamgoue, Marc Stadler, et al.
Phytochemical Analysis : PCA|November 3, 2023
Discovery and characterisation of a broderol-like illudin, omphaderol in the mycelial extracts of Omphalotus mexicanus (Omphalotaceae) using UPLC-QTOF-MS and NMR spectroscopyPaul Eckhardt, Silke Reinecke, Till Opatz, et al.
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